首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 31 毫秒
1.
2.
We address several conjectures raised in Cantrell et al. [Evolution of dispersal and ideal free distribution, Math. Biosci. Eng. 7 (2010), pp. 17–36 [9 Cantrell, R. S., Cosner, C. and Lou, Y. 2010. Evolution of dispersal and ideal free distribution. Math. Biosci. Eng., 7: 1736. [Crossref], [PubMed], [Web of Science ®] [Google Scholar]]] concerning the dynamics of a diffusion–advection–competition model for two competing species. A conditional dispersal strategy, which results in the ideal free distribution of a single population at equilibrium, was found in Cantrell et al. [9 Cantrell, R. S., Cosner, C. and Lou, Y. 2010. Evolution of dispersal and ideal free distribution. Math. Biosci. Eng., 7: 1736. [Crossref], [PubMed], [Web of Science ®] [Google Scholar]]. It was shown in [9 Cantrell, R. S., Cosner, C. and Lou, Y. 2010. Evolution of dispersal and ideal free distribution. Math. Biosci. Eng., 7: 1736. [Crossref], [PubMed], [Web of Science ®] [Google Scholar]] that this special dispersal strategy is a local evolutionarily stable strategy (ESS) when the random diffusion rates of the two species are equal, and here we show that it is a global ESS for arbitrary random diffusion rates. The conditions in [9 Cantrell, R. S., Cosner, C. and Lou, Y. 2010. Evolution of dispersal and ideal free distribution. Math. Biosci. Eng., 7: 1736. [Crossref], [PubMed], [Web of Science ®] [Google Scholar]] for the coexistence of two species are substantially improved. Finally, we show that this special dispersal strategy is not globally convergent stable for certain resource functions, in contrast with the result from [9 Cantrell, R. S., Cosner, C. and Lou, Y. 2010. Evolution of dispersal and ideal free distribution. Math. Biosci. Eng., 7: 1736. [Crossref], [PubMed], [Web of Science ®] [Google Scholar]], which roughly says that this dispersal strategy is globally convergent stable for any monotone resource function.  相似文献   

3.
ABSTRACT

Discovered in 1954 by Ambroggi and Lapparent, the Tagragra tracksite (Maastrichtian, Agadir, Morocco) yielded tracks of theropod dinosaurs, birds and enigmatic forms tentatively attributed to Lacertilia under the name Agadirichnus elegans. The original specimens are today considered to be lost, and the status of A. elegans has been questioned, even though these footprints can retrospectively be referred to pterodactyloid pterosaur tracks. In order to discuss the status of these foot prints, the historical site has been actively sought and recently rediscovered by one of us (MdD). New material confirms the presence of pterodactyloid footprints, with two morphotypes, in two different facies, respectively associated with bird and theropod tracks. Morphotype I is tentatively conferred to Pteraichnus Stokes 1957 Stokes, W. L. 1957. Pterodactyl tracks from the Morrison Formation. Journal of Palaeontology, 31:9524.[Web of Science ®] [Google Scholar], which extends the stratigraphical distribution of this ichnotaxon to the Maastrichtian. Morphotype II corresponds to the original ichnospecies A. elegans Ambroggi and Lapparent 1954 Ambroggi, R., and A. F. de Lapparent 1954. Les empreintes de pas fossiles du Maestrichtien d'Agadir. Notes du Service Géologique du Maroc, 10:436. [Google Scholar], which is here reassessed as a valid ichnotaxon, with the designation of a neotype. Thus, A. elegans Ambroggi and Lapparent 1954 Ambroggi, R., and A. F. de Lapparent 1954. Les empreintes de pas fossiles du Maestrichtien d'Agadir. Notes du Service Géologique du Maroc, 10:436. [Google Scholar] is historically the first pterosaurian ichnotaxon ever described.  相似文献   

4.
Abstract

A new ichnofossiliferous locality in Salta Province (northwest Argentina) contains an association with numerous irregular spiral traces assigned to Spirodesmos milanai n. isp., in mature sandstones and quartzites with rippled bedding surfaces, rare wavy lamination and cross-bedded stratification. This record of early spiral behavior is interpreted as a primitive grazing method formed on muddy laminae above sand layers, and is related to a feeding strategy of an annelid-type of organism. Associated traces are Cruziana cf. semiplicata, Diplocraterion isp., Monocraterion isp., Rusophycus isp., Skolithos linearis Haldeman and Skolithos magnus Howell. The ichnoassemblage is similar to a shallow-water ichnoassociation from the Permian Ecca Group of South Africa (Mason et al., 1983 Mason, T. R., Stanistreet, I. G. and Tavener-Smith, R. 1983. Spiral trace fossils from the Permian Ecca Group of Zululand. Lethaia, 16: 241247. [Crossref], [Web of Science ®] [Google Scholar]).  相似文献   

5.
The species of genus Antillophos Woodring, 1928 Woodring, W.P. (1928) Miocene Mollusks from Bowden, Jamaica. 2. Gastropods and Discussion of Results. Contributions to the Geology and Paleontology of the West Indies. Carnegie Institute of Washington, Washington D.C. [Google Scholar] from the China seas are studied. Six species, Antillophos liui n. sp., Antillophos lucubratonis Fraussen & Poppe, 2005 Fraussen, K. & Poppe, G.T. (2005) Revision of Phos and Antillophos (Buccinidae) from the Central Philippines. Visaya 1, 76115. [Google Scholar], Antillophos monsecourorum Fraussen & Poppe, 2005 Fraussen, K. & Poppe, G.T. (2005) Revision of Phos and Antillophos (Buccinidae) from the Central Philippines. Visaya 1, 76115. [Google Scholar], Antillophos pyladeum (Kato, 1995 Kato, S. (1995) Discussion of the genus Phos. Hitaciobi 70, 1520. [Google Scholar]), Antillophos roseatus (Hinds, 1844 Hinds, R.B. (1844) Mollusca. In: Hinds, R.B. (Ed.) The Zoology of the Voyage of H.M.S. Sulphur During the years 18361842. 2. Smith, Elder and Co., London, pp. 172. [Google Scholar]) and Antillophos sp., are described and illustrated.

http://zoobank.org/urn:lsid:zoobank.org:pub:51481997-A841-4F37-8E15-B753DC99CB4D  相似文献   

6.
The Divakar-Reese procedure has been successfully applied for transforming 7-oxo-isothiazolo[4,5-d]pyrimidine C-nucleosides (4a,b, 5a,b, 6a) via 1,2,4-triazol-1-yl intermediates (7a,b, 8a,b) into various 7-substituted C-nucle- osides 15a,b, 16a,b, 17a, 18a, 19a,b, 20a,b; their subsequent deprotection provides novel types of unusual C-glycosides 22b, 23a, 24a,b, 25b, 26b.

C-Nucleosides, possessing on its heterocyclic base other than naturally occuring oxo- or amino substituents, are important model compounds for biological or medicinal studies [2a] Hanessian, S. and Pernet, A. G. 1976. Adv. Carbohydr. Chem. Biochem., 32: 111188. cf. [Google Scholar], [2b] Mizuno, Y. 1986. The Organic Chemistry of Nucleic Acids Amsterdam: Elsevier.  [Google Scholar], [2c] Huryn, D. M. and Okabe, M. 1992. Chem. Rev., 92: 17451768. [Crossref], [Web of Science ®] [Google Scholar], [2d] Häbich, D. 1991. Chem. in uns. Zeit, 25: 295307.  [Google Scholar], [2e] Uhlmann, E. and Peyman, A. 1990. Chem. Rev., 90: 543584. [Crossref], [Web of Science ®] [Google Scholar], [2f] Thuong, N. T. and Helene, C. 1993. Angew. Chem., 105: 697723. [Crossref] [Google Scholar], [2g] 1993. Angew. Chem. Int. Ed. Engl., 33: 666690.  [Google Scholar], [2h] Yarchoan, R., Mitsuya, H., Zhomas, R. V., Pluda, J. M., Hartman, N. R., Perno, C. F., Marczyk, K. S., Allain, J. P., Johns, D. G. and Broder, S. 1989. Science, 245: 412414. [Crossref], [PubMed], [Web of Science ®] [Google Scholar], [2i] Tanaka, H., Baba, M., Hayakawa, H., Sakamaki, T., Miyasaka, T., Ubasawa, M., Takashima, H., Sekiya, E., Nitta, I., Shigeta, S., Walker, R. T., Balzarini, J. and De Clerq, E. 1991. J. Med. Chem., 34: 349357. [Crossref], [PubMed], [Web of Science ®] [Google Scholar] [3a] Koyama, G., Maeda, K., Umezawa, H. and Iitaka, Y. 1966. Tetrahedron Lett., : 597602. Some C-glycosides with antibiotic, antiviral (HIV), and anticancer activities [Google Scholar], [3b] Hori, M., Wakashiro, T., Ito, E., Sawa, T., Takeuchi, T. and Umezawa, H. J. 1968. J. Antibiot., 21A: 264270. [Chem. Abstr. 1968, 69, 11356j] [Google Scholar], [3c] Farkas, J. and ?orm. 1972. F. Collect. Czech. Chem. Commun., 37: 27982803.  [Google Scholar], [3d] Acton, E. M., Ryan, K. J., Henry, D. W. and Goodman, L. 1971. J. Chem. Soc., Chem. Commun., : 986988.  [Google Scholar], [3e] Nakagawa, Y., Kano, H., Tsukuda, Y. and Koyama, H. 1967. Tetrahedron Lett., : 41054109.  [Google Scholar], [3f] Inoue, I. and Kuwaijama, I. 1980. J. Chem. Soc., Chem. Commun., : 251253.  [Google Scholar], [3g] Buchanan, J. G., Stobie, A. and Wightman, R. H. 1980. ibid., : 916917. [Crossref] [Google Scholar], [3h] Hildebrand, S. and Leumann, C. 1996. Angew. Chem., 108: 21002102. Angew. Chem. Int. Ed. Engl. 1996, 35, 1968–1970 [Google Scholar]. We want to report on the synthesis of novel 7-substituted isothiazolo = [4,5-d]pyrimidine C-nucleosides. As we could show in previous papers [1] Wamhoff, H., Berressem, R. and Nieger, M. 1994. J. Org. Chem., 59: 19121917. Part 2 [Google Scholar], [4] Wamhoff, H., Berressem, R. and Nieger. 1993. M. J. Org. Chem., 58: 51815185.  [Google Scholar], there exists a simple approach to the protected C-glycosides 46.

  相似文献   

7.
8.
Four new species of the subgenus Stegana (sensu stricto) were found and described from China: S. (S.) antha sp. nov., S. (S.) latiorificia sp. nov., S. (S.) huangjiai sp. nov. and S. (S.) nigrifoliacea sp. nov. Three known Stegana (s. str.) species from China: S. (S.) antlia Okada, 1991, S. (S.) cheni Sidorenko, 1997 Sidorenko, V. S. (1997). New Asian species and new records of the genus Stegana Meigen (Diptera, Drosophilidae). I. Subgenera Oxyphortica Duda and Stegana s. str. Annales d la Société Entomologique de France (N. S.), 33, 6579.[Web of Science ®] [Google Scholar] and S. (S.) emeiensis Sidorenko, 1997 Sidorenko, V. S. (1997). New Asian species and new records of the genus Stegana Meigen (Diptera, Drosophilidae). I. Subgenera Oxyphortica Duda and Stegana s. str. Annales d la Société Entomologique de France (N. S.), 33, 6579.[Web of Science ®] [Google Scholar] are redescribed as supplementary information. A key to the species, based on morphological characters, is provided. The phylogenetic relationships among 14 species of the subgenus Stegana are reconstructed with the combined sequences of the mitochondrial genes, ND2 (NADH dehydrogenase subunit 2) and COI (cytochrome c oxidase, subunit I). Moreover, the intra- and interspecific pairwise K-2P (Kimura's two-parameter) distances among these species are summarized, and the availability of mitochondrial markers in the species identification of the subgenus Stegana are further discussed.

http://www.zoobank.org/urn:lsid:zoobank.org:pub:368C55C3-B101-457C-BD61-BDD8F1B780E5  相似文献   

9.
This study investigates the diversity and taxonomy of a mainly marine group of species lacking chaetae currently assigned to the genus Marionina. This achaetous group includes four nominal species: M. achaeta (Hagen, 1954 Hagen, G. 1954. Michaelsena achaeta nov. sp., ein neuer mariner Oligochaet aus der Kieler Bucht. Faunistische Mitteilungen aus Norddeutschland, 1: 1213.  [Google Scholar]), M. achaeta sensu Lasserre, 1964 Lasserre, P. 1964. Notes sur quelques oligochètes Enchytraeidae présents dans les plages du Bassin d’Arcachon. Procés-Verbaux des Séances de la Société Linnéenne de Bordeaux, 101: 8791.  [Google Scholar], M. nevisensis Righi & Kanner, 1979 Righi, G. and Kanner, E. 1979. Marine Oligochaeta (Tubificidae and Enchytraeidae) from the Caribbean Sea. Studies of the Fauna of Curaçao and other Caribbean Islands, 58: 4468.  [Google Scholar] and M. arenaria Healy, 1979 Healy, B. 1979a. Marine fauna of County Wexford. 1 – Littoral and brackishwater Oligochaeta. The Irish Naturalists' Journal, 19: 418422.  [Google Scholar]. As Lasserre's (1964 Lasserre, P. 1964. Notes sur quelques oligochètes Enchytraeidae présents dans les plages du Bassin d’Arcachon. Procés-Verbaux des Séances de la Société Linnéenne de Bordeaux, 101: 8791.  [Google Scholar]) M. achaeta appears to be morphologically different from its (then) senior homonym M. achaeta (Hagen, 1954 Hagen, G. 1954. Michaelsena achaeta nov. sp., ein neuer mariner Oligochaet aus der Kieler Bucht. Faunistische Mitteilungen aus Norddeutschland, 1: 1213.  [Google Scholar]), the replacement name M. nothachaeta nom. nov. is proposed for it. We studied the genetic and morphological diversity of achaetous specimens of Marionina collected in Florida, the Great Barrier Reef, New Caledonia, Sweden, England and the Bahamas. The collection localities are almost all supralittoral and often brackish-water habitats. Parts of the mitochondrial genes 12S, 16S, COI and the nuclear genes 18S, 28S and ITS were analysed to assess the genetic variation and phylogeny of the achaetous Marionina species. The molecular data reveal one monophyletic group of 11 separately evolving lineages, and between these lineages, K2P distances in the barcoding gene COI vary between 5.4 and 25.0%. On a morphological basis, the lineages could be assigned to seven different groups (morphotypes), of which only two could be identified as described nominal taxa: M. nevisensis s. lat. (several lineages) and M. nothachaeta. Since the former taxon appears to be a complex of cryptic species around the world and the original type material no longer exists, a neotype from the Caribbean was designated for M. nevisensis s. str. The remaining achaetous lineages represent five morphologically distinct species that are left unnamed, awaiting finer morphological scrutiny and detailed comparisons with new collections of M. achaeta and M. arenaria. Summing up, the group of achaetous Marionina now seems to contain up to 13 different species, seven of which are yet to be formally described and named.  相似文献   

10.
Two new harvestmen species of the family Phalangiidae, Rilaena caucasica sp. n. and Rilaena silhavyi sp. n. are diagnosed, illustrated, and described from the Caucasus region. Comparative illustration of the related Rilaena anatolica (Roewer, 1956), R. atrolutea (Roewer, 1915) and R. kelbajarica Snegovaya &; Pkhakadze, 2014 Snegovaya, N. Y., &; Pkhakadze, V. D. (2014): New species of the genus Rilaena (Opiliones, Phalangiidae) from the mount Gyamish, Azerbaijan. Vestnik zoologii, 48, 313318. doi: 10.2478/vzoo-2014-0037[Crossref] [Google Scholar] are given.

http://www.zoobank.org/urn:lsid:zoobank.org:pub:7B29FD94-45A2-4E32-A41E-3276E016410B  相似文献   

11.
12.
Five species of the genus Catomus Allard, 1876 Allard, E. (1876): Révision des Helopines vrais de Lacordaire. L'Abeille. Journal d'Entomologie, 14, 180. [Google Scholar] are known from Iran. Catomus fragilis (Ménétriés, 1848) is recorded from Iran for the first time. Lectotypes of C. persicus Allard, 1876 Allard, E. (1876): Révision des Helopines vrais de Lacordaire. L'Abeille. Journal d'Entomologie, 14, 180. [Google Scholar] (type species of the genus) and C. semiruber Allard, 1876 Allard, E. (1876): Révision des Helopines vrais de Lacordaire. L'Abeille. Journal d'Entomologie, 14, 180. [Google Scholar] are designated. These species are also redescribed and figured. A key to the species of Catomus in the Iranian fauna is given.  相似文献   

13.
The new materials of carbon, solid C60 and carbon nanotubes (CNT) [1 Chesnokov, S.A., Nalimova, V.A., Rinzler, A.G., Smalley, R.E. and Fischer, E. 1999. Mechanical energy storage in carbon nanotube springs. PRL, 82: 343[Crossref], [Web of Science ®] [Google Scholar],4 V.K. Jindal, Shuchi Gupta, K. Dharamvir, Bulk and lattice properties for rigid carbon nanotubes materials. http://arxiv.org/abs/cond-mat/0008382  [Google Scholar]] are important for various technological applications. One of the reasons for their technological applications could be based upon the fact that they have a lot of empty space in their molecules as well as in their unit cells when bulk quantities of these are taken in the form of either C60 solid or nanoropes. Their compressibility studies have revealed extremely interesting results showing tremendous reversible compression which has aroused curiosity and interest. CNT have been found to be compressible reversibly up to about 65% of their original volume when subjected to pressures of about 20 kbar. This enormous volume compression in such materials under moderate pressures is conceived to be of great significance for understanding and interpreting the mechanism based on molecular level understanding related to shock compression in these materials.

We undertake a model study accounting for unit cell deformations by applying pressures up to 3 Gpa and develop a pressure compression relation. We use the anharmonicity of the intermolecular potential energy to calculate Gruneisen parameters and the temperature increase due to an adiabatic pressure application. This work uses some components calculated from a rigid molecule model, whereas others are taken from experimental pressure compression data.  相似文献   

14.
Recent adaptationist accounts of human mental and physical health have reinvigorated the debate over the evolution of human intelligence. In the tradition of strong inference the current study was developed to determine whether either Miller's (1998 Miller, G. F. 1998. “How mate choice shaped human nature: A review of sexual selection and human evolution”. In Handbook of evolutionary psychology: Ideas, issues, and applications, Edited by: Crawford, C. and Krebs, D. 87129. Hillsdale, NJ: Lawrence Erlbaum.  [Google Scholar], 2000a Miller, G. F. 2000a. Mental traits as fitness indicators: Expanding evolutionary psychology's adaptationism. Evolutionary approaches to human reproductive behavior. Ann N Y Acad Sci, 907: 6274. [Crossref], [PubMed], [Web of Science ®] [Google Scholar]) Fitness Indicator Theory or Rushton's (1985 Rushton, J. P. 1985. Differential K theory: The sociobiology of individual and group differences. Pers Indiv Diff, 6(4): 441452. [Crossref] [Google Scholar], 2000 Rushton, J. P. 2000. Race, evolution, and behavior: A life-history perspective, 3rd, Port Huron, MI: Charles Darwin Research Institute.  [Google Scholar]) Differential-K Theory better accounts for general intelligence (“g”) in an undergraduate university population (N = 192). Owing to the lengthy administration time of the test materials, a newly developed 18-item short form of the Ravens Advanced Progressive Matrices (APM-18; Sefcek, Miller, and Figueredo 2007 Sefcek, J. A., Miller, G. F. and Figueredo, A. J. 2007. “Development and of an 18-item short form of the Ravens Advanced Progressive Matrices (RAPM-18). (Submitted)”.  [Google Scholar]) was used. A significant, positive relationship between K and F (r = .31, p < .001) emerged. Contrary to predictions, no significant relationships were found between “g” and either K or F (r = –.09, p ≥ .05 and r = .11, p ≥ .05, respectively). Though generally contrary to both hypotheses, these results may be explained in relation to antagonistic pleiotropy and a potential failure to derive correct predictions for within-species comparisons directly from the results of between-species comparisons.  相似文献   

15.
16.
The Oriental Region harbours the second richest fauna of freshwater bivalves in the world, including many endangered endemic taxa. However, the Oriental fauna of the Unionidae have been very poorly studied using an integrative taxonomic approach, which may provide reasonable revisions of complicated (cryptic) taxa based on morphological, molecular, biogeographic and ecological evidence. Here, we present the first example of an integrative taxonomic revision concerning the status of Unio exolescens Gould (1843 Gould, A.A. (1843). Dr. Gould had examined the shells not long since announced as having been received from the Rev. Francis Mason, missionary at Tavoy, in British Burmah. Proceedings of the Boston Society of Natural History, 1, 139141. [Google Scholar]), a nominal mussel taxon that was accepted as a valid species within the genus Trapezoideus Simpson (1900). Currently, Trapezoideus exolescens is considered the type of the genus as far as the originally designated type species, U. foliaceus Gould (1843 Gould, A.A. (1843). Dr. Gould had examined the shells not long since announced as having been received from the Rev. Francis Mason, missionary at Tavoy, in British Burmah. Proceedings of the Boston Society of Natural History, 1, 139141. [Google Scholar]), was considered to be a synonym of T. exolescens. Using nucleotide sequences obtained from mitochondrial (COI and 16S rRNA) and nuclear (28S rDNA) genes, we found that the topotypes of Unio exolescens Gould (1843 Gould, A.A. (1843). Dr. Gould had examined the shells not long since announced as having been received from the Rev. Francis Mason, missionary at Tavoy, in British Burmah. Proceedings of the Boston Society of Natural History, 1, 139141. [Google Scholar]) cluster together with representatives of another mussel genus, Lamellidens Simpson (1900). Based on these results and on morphological data, we transfer Unio exolescens Gould (1843 Gould, A.A. (1843). Dr. Gould had examined the shells not long since announced as having been received from the Rev. Francis Mason, missionary at Tavoy, in British Burmah. Proceedings of the Boston Society of Natural History, 1, 139141. [Google Scholar]) from Trapezoideus to Lamellidens and propose Lamellidens exolescens (Gould, 1843 Gould, A.A. (1843). Dr. Gould had examined the shells not long since announced as having been received from the Rev. Francis Mason, missionary at Tavoy, in British Burmah. Proceedings of the Boston Society of Natural History, 1, 139141. [Google Scholar]) comb. nov. In addition, we revisited the status of Unio foliaceus Gould (1843 Gould, A.A. (1843). Dr. Gould had examined the shells not long since announced as having been received from the Rev. Francis Mason, missionary at Tavoy, in British Burmah. Proceedings of the Boston Society of Natural History, 1, 139141. [Google Scholar]) as a valid species and the type of the genus Trapezoideus based on the morphological study of the type specimen, although a question concerning the true position of this taxon is still open because its molecular sequences are not available. Our findings highlight that an integrative taxonomic approach is an important tool, particularly when dealing with such species-rich Unionidae fauna as those of the Oriental Realm.  相似文献   

17.
This paper contains a taxonomic study of the Permian tetrapod ichnofauna from the Carapacha Basin. Tetrapod traces are analyzed in their environmental context and compared with similar faunas from Europe and North America. This ichnofauna is particularly relevant because of the scarcity of Permian tetrapod tracks from South America and also of Permian tetrapod fossils from Argentina. Ephemeral fluvial and shallow lacustrine deposits compose the sedimentary succession of the basin, which is represented by the Carapacha Formation. Most of the tracks have been collected from the upper member of the formation (Urre-Lauquen Member), mainly from freshwater ephemeral lake deposits as well as from playa-lake mudflats. The deposits of this member have been attributed to the early Late Permian on the basis of a Glossopteris fossil flora. Ichnotaxonomic designations of tetrapod traces are made on the basis of morphologic features that reflect the anatomy of the producer and special attention has been paid to extramorphologic deformations observed in the track assemblage. A total of four footprint ichnotaxa have been recognized, namely Batrachichnus salamandroides (Geinitz, 1861 Geinitz, H. B. 1861. Dyas oder die Zechsteinformation und das Rhotliegende—Die animalischen Überreste der Dyas, 130 ppLeipzig: Wilhelm Engelmann.  [Google Scholar]), Hyloidichnus bifurcatus Gilmore, 1927 Gilmore, C. W. 1927. Fossil footprints from the Grand Canyon: second contribution. Smithsonian Miscellaneous Collection, 80(3): 178.  [Google Scholar], cf. Amphisauropus isp. and cf. Varanopus isp. These track taxa are associated with two forms of vertebrate swimming traces (Characichnos isp. and type A swimming trace) and a possible fish trail. Invertebrate trace fossils include abundant arthropod locomotion traces and Scoyenia isp. The ichnofauna is composed of six tetrapod ichnocoenoses that are dominated by tiny amphibian tracks attributed to Temnospondyli (Batrachichnus and type A swimming trace) and Seymouriamorpha (Amphisauropus), and also contain the footprints of small reptiles, mostly Captorhinomorpha and possibly Pelycosauria (Hyloidichnus and Varanopus). Even if the ichnofauna of the Carapacha Basin is slightly younger than typical examples from the literature of the Early Permian “red bed ichnofacies” (Hunt et al., 1995b Hunt, A. P., Lucas, S. G., Lockley, M. G., Haubold, H. and Braddy, S. 1995b. Tetrapod ichnofacies in Early Permian red beds of the American Southwest. Bulletin New Mexico Museum of Natural History and Science, 6: 295301. Early Permian footprint facies [Google Scholar]), a comparison is made. However, further detailed case studies are needed to formally define this “red bed ichnofacies” and its prospective subdivisions.  相似文献   

18.
19.
Cajus Diedrich 《Ichnos》2013,20(3-4):215-228
This article examines the high-resolution track horizon stratigraphy at the outcrop Obernkirchen. Massive sandstones, products of marine sand bar and fluviatile environments are present at the tracksite. Recently two track beds were examined in the outcrop. One new track slab of the lower track bed is described exposing well-preserved quadrupedal iguanodontid tracktypes of Iguanodontipus Sarjeant, Delair, and Lockley, 1998 Sarjeant, W. A. S., Delair, J. B. and Lockley, M. G. 1998. The footprints of Iguanodon: a history and taxonomic study. Ichnos, 6: 183202. [Taylor & Francis Online] [Google Scholar], and bipedal theropod tracks Megalosauropus Kaever and Lapparent, 1974 Kaever, M. and Lapparent, A. F. de. 1974. Les traces des pas le Dinosaures du Jurassique des Barkhausen (Basse Saxe, Allemagne). Bulletin de la Societé Geologique Français, 16: 516525.  [Google Scholar]. The ichnogenus Iguanodontipus is discussed and the diagnosis extended. The tracksite Obernkirchen belongs to a megatracksite of the ancient coastline of the marginal marine Hercynic Basin of the Lower Cretaceous of Europe, including the four well-known sites Obernkirchen, Bad Rehburg, Münchehagen, and Bückeburg of Northwest Germany. Three different tracktypes of huge sauropods, theropods, and ornithopods are abundant at basal Lower Cretaceous siliciclastic coastlines in different regions in Spain, Portugal, England, Germany, and Switzerland. Dinosaur tracks are also present in carbonate platform environments of northern Italy and Istria.  相似文献   

20.
Abstract

The checklist comprises all species of six families of Iranian aquatic Polyphaga (Coleoptera). In total, 43 species/subspecies within the families, Georissidae (one species), Helophoridae (25 species and two subspecies), Hydrochidae (three species), Spercheidae (one species), Curculionidae (nine species) and Erirhinidae (two species) are listed for the fauna of Iran. Helophorus (Rhopalohelophorus) nanus Sturm, 1836 Sturm, J. (1836), Deulschlands Fauna in Abbildungen nach der Natur mit Beschreibungen. V. Abtheilung. Die Inseclen. Zehntes Bändchen. Käfer, Nürnberg: J. Sturm, 108 pp., pl. 216–227. (also under title: Deutschlands Insecten, Käfer). [Google Scholar] (Helophoridae) is recorded for the first time from Iran. We also present two additional species lists: one with incorrect records (one species) and the other with unidentified species.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号